rs10877839
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10877839(C;C) |
Make rs10877839(C;T) |
Make rs10877839(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 62424701 |
is a | snp |
is | mentioned by |
dbSNP | rs10877839 |
dbSNP (classic) | rs10877839 |
ClinGen | rs10877839 |
ebi | rs10877839 |
HLI | rs10877839 |
Exac | rs10877839 |
Gnomad | rs10877839 |
Varsome | rs10877839 |
LitVar | rs10877839 |
Map | rs10877839 |
PheGenI | rs10877839 |
Biobank | rs10877839 |
1000 genomes | rs10877839 |
hgdp | rs10877839 |
ensembl | rs10877839 |
geneview | rs10877839 |
scholar | rs10877839 |
rs10877839 | |
pharmgkb | rs10877839 |
gwascentral | rs10877839 |
openSNP | rs10877839 |
23andMe | rs10877839 |
SNPshot | rs10877839 |
SNPdbe | rs10877839 |
MSV3d | rs10877839 |
GWAS Ctlg | rs10877839 |
GMAF | 0.3021 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23382691] |
Trait | IgG glycosylation |
Title | Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers. |
Risk Allele | C |
P-val | 9E-6 |
Odds Ratio | .15 [0.082-0.21] unit decrease |
Categories:
- Is a snp
- In dbSNP
- SNPs on chromosome 12
- Has genotype
- Has population
- On chip 23andMe v1
- On chip 23andMe v2
- On chip 23andMe v3
- On chip 23andMe v4
- On chip Affy GenomeWide 6
- On chip Ancestry v2
- On chip FTDNA2
- On chip FTDNA
- On chip HumanOmni1Quad
- On chip Illumina Human 1M
- On chip NatGeo2
- On chip 23andMe v5
- On chip Ancestry v2c
- On chip Ancestry v2d